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Variant : CV601783 (GRCh37/hg19 7q34-36.3(chr7:141938235-159126310)x1) Homo sapiens

Symbol: CV601783
Name: GRCh37/hg19 7q34-36.3(chr7:141938235-159126310)x1
Condition: not provided [RCV000747083]
Clinical Significance: pathogenic
Last Evaluated: 11/12/2013
Review Status: no assertion criteria provided
Related Genes: ABCB8   ABCF2   ACTR3B   ACTR3C   AGAP3   AOC1   ARHGEF35   ARHGEF5   ASB10   ASIC3   ATG9B   ATP6V0E2   C7orf33   CASP2   CDK5   CHPF2   CLCN1   CNPY1   CNTNAP2   CRYGN   CTAGE15   CTAGE4   CTAGE6   CTAGE8   CUL1   DNAJB6   EN2   EPHA1   EPHB6   ESYT2   EZH2   FAM131B   FASTK   GALNT11   GALNTL5   GBX1   GIMAP1   GIMAP2   GIMAP4   GIMAP5   GIMAP6   GIMAP7   GIMAP8   GSTK1   HTR5A   INSIG1   KCNH2   KEL   KMT2C   KRBA1   LLCFC1   LMBR1   LRRC61   MIR671   MNX1   MTRNR2L6   NCAPG2   NOBOX   NOM1   NOS3   NUB1   OR2A1   OR2A12   OR2A14   OR2A2   OR2A25   OR2A42   OR2A5   OR2A7   OR2F1   OR2F2   OR6B1   OR6V1   OR9A2   PAXIP1   PDIA4   PIP   PRKAG2   PRSS1   PRSS58   PTPRN2   RARRES2   RBM33   REPIN1   RHEB   RNF32   RNY1   RNY3   RNY4   RNY5   SHH   SLC4A2   SMARCD3   TAS2R39   TAS2R40   TAS2R41   TAS2R60   TCAF1   TCAF2   TMEM139   TMEM176A   TMEM176B   TMUB1   TPK1   TRB   TRPV5   TRPV6   UBE3C   VIPR2   WDR60   WDR86   XRCC2   ZBED6CL   ZNF212   ZNF282   ZNF398   ZNF425   ZNF467   ZNF746   ZNF775   ZNF777   ZNF783   ZNF786   ZNF862   ZYX  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh377141,938,235 - 159,126,310CLINVAR
Cytogenetic Map77q34-36.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14362430
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.